APOLIPOPROTEIN E4 GENOTYPE IS NOT A RISK FACTOR FOR SYSTEMIC AA AMYLOIDOSIS OR FAMILIAL AMYLOID POLYNEUROPATHY

被引:12
作者
LOVAT, LB
BOOTH, SE
BOOTH, DR
MADHOO, S
HOLMGREN, G
HAWKINS, PN
SOUTAR, AK
PEPYS, MB
机构
[1] HAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,DEPT MED,IMMUNOL MED UNIT,LONDON W12 0NN,ENGLAND
[2] HAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,CTR CLIN SCI,MRC LIPOPROT TEAM,LONDON W12 0NN,ENGLAND
[3] UMEA UNIV HOSP,DEPT CLIN GENET,S-90185 UMEA,SWEDEN
来源
AMYLOID-INTERNATIONAL JOURNAL OF EXPERIMENTAL AND CLINICAL INVESTIGATION | 1995年 / 2卷 / 03期
基金
英国医学研究理事会;
关键词
APOLIPOPROTEIN E; AA AMYLOIDOSIS; FAMILIAL AMYLOID POLYNEUROPATHY;
D O I
10.3109/13506129509036920
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Apolipoprotein E (apoE) is present in the amyloid deposits in Alzheimer's disease (AD) and in acquired and hereditary systemic amyloidosis, and apoE genotype is an important risk factor for late onset AD. In order to determine whether it is also a risk factor for developing reactive systemic amyloid A protein (AA) amyloidosis or transthyretin (TTR) Met 30 familial amyloid polyneuropathy (FAP), apoE genotype was determined in 32 patients with AA amyloid and 31 patients with FAP. Prevalence of the apoE epsilon 4 allele was not significantly different than in a normal population. There was also no correlation between apoE genotype and either the time from presentation of the underlying disease to the diagnosis of AA amyloid or the age of onset of symptoms in FAP These results suggest that apoE genotype does not affect susceptibility to or expression of AA amyloidosis or TTR Met 30 FAP.
引用
收藏
页码:163 / 166
页数:4
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